材料科学
阳极
电解质
金属锂
锂(药物)
电镀(地质)
堆栈(抽象数据类型)
磷酸钒锂电池
金属
化学工程
电极
冶金
化学
医学
工程类
物理化学
计算机科学
程序设计语言
内分泌学
地球物理学
地质学
作者
Jean‐Marie Doux,Nguyen, Han,Darren H. S. Tan,Abhik Banerjee,Xuefeng Wang,Erik A. Wu,Chiho Jo,Hedi Yang,Ying Shirley Meng
标识
DOI:10.1002/aenm.201903253
摘要
Abstract All‐solid‐state batteries are expected to enable batteries with high energy density with the use of lithium metal anodes. Although solid electrolytes are believed to be mechanically strong enough to prevent lithium dendrites from propagating, various reports today still show cell failure due to lithium dendrit growth at room temperature. While cell parameters such as current density, electrolyte porosity, and interfacial properties have been investigated, mechanical properties of lithium metal and the role of applied stack pressure on the shorting behavior are still poorly understood. Here, failure mechanisms of lithium metal are investigated in all‐solid‐state batteries as a function of stack pressure, and in situ characterization of the interfacial and morphological properties of the buried lithium is conducted in solid electrolytes. It is found that a low stack pressure of 5 MPa allows reliable plating and stripping in a lithium symmetric cell for more than 1000 h, and a Li | Li 6 PS 5 Cl | LiNi 0.80 Co 0.15 Al 0.05 O 2 full cell, plating more than 4 µm of lithium per charge, is able to cycle over 200 cycles at room temperature. These results suggest the possibility of enabling the lithium metal anode in all‐solid‐state batteries at reasonable stack pressures.
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